HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2,4-dimethoxy-5-nitrobenzoate → Methyl 5-amino-2,4-dimethoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2,4-dimethoxy-5-nitrobenzoate | HCID 11622839 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 5-amino-2,4-dimethoxybenzoate | HCID 16638096 | — |
Reaction Steps
A 4.00 g portion of methyl 2,4-dimethoxy-5-nitrobenzoate was dissolved in 200 ml of tetrahydrofuran, and 0.40 g of 10% palladium-carbon was added, followed by stirring for 12 hours at room temperature under normal pressure in an atmosphere of hydrogen. After removing insoluble matter by filtration, the solvent was evaporated under a reduced pressure to give 3.6 g of methyl 5-amino-2,4-dimethoxybenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05686482 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-fdf582eeabdf4a26ba561139d65a47bb |
| Source note | uspto-grants-1997_11 |